HW 10 #7 **Instruction for Educational Website:**Click the "draw structure" button to launch the drawing utility.Draw the constitutional isomer formed in the following reaction.**Diagram Explanation:**The image depicts a chemical reaction starting with cyclohexylmethane (a hexagon representing cyclohexane with a CH₂ group attached). 1. The first reagent used in the reaction is 9-BBN (9-Borabicyclo[3.3.1]nonane).2. The second step involves H₂O₂ (hydrogen peroxide) and HO⁻ (hydroxide ion).The arrow indicates that these reagents react with the starting compound. Users are instructed to draw the resulting constitutional isomer using a drawing utility by clicking the "edit structure..." button. This reaction typically suggests hydroboration-oxidation, where an alkene (if one were present) would be transformed into an alcohol. However, details of this reaction specifically would be determined by the context of the complete molecular structure.

9-BBN is known as 9-Borabicyclo(3.3.1)nonane9-Borabicyclo[3.3.1]nonane or 9-BBN is an organoborane compound, used as a hydroboration reagent. The compound exists as a hydride-bridged dimer and also known by its nickname 'banana borane'. For convenience we can use the term R2BH for 9-BBN.The methylenecyclohexane will react with banana borane to form the organoborane compound, this compound is formed on the terminal end as the backside of the alkene is blocked by the cyclohaxane moiety. In the presence of basic condition the organoborane will hydrolyse to give the corresponding alcohol.